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Sub-Chronic Microcystin-LR Liver Toxicity in Preexisting Diet-Induced Nonalcoholic Steatohepatitis in Rats

机译:亚慢性微囊藻毒素-LR肝毒性在预先存在的饮食诱导大鼠非酒精性脂肪性肝炎中

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摘要

Microcystin-LR (MCLR) is a hepatotoxic cyanotoxin reported to cause a phenotype similar to nonalcoholic steatohepatitis (NASH). NASH is a common progressive liver disease that advances in severity due to exogenous stressors such as poor diet and toxicant exposure. Our objective was to determine how sub-chronic MCLR toxicity affects preexisting diet-induced NASH. Sprague-Dawley rats were fed one of three diets for 10 weeks: control, methionine and choline deficient (MCD), or high fat/high cholesterol (HFHC). After six weeks of diet, animals received vehicle, 10 µg/kg, or 30 µg/kg MCLR via intraperitoneal injection every other day for the final 4 weeks. Incidence and severity scoring of histopathology endpoints suggested that MCLR toxicity drove NASH to a less fatty and more fibrotic state. In general, expression of genes involved in de novo lipogenesis and fatty acid esterification were altered in favor of decreased steatosis. The higher MCLR dose increased expression of genes involved in fibrosis and inflammation in the control and HFHC groups. These data suggest MCLR toxicity in the context of preexisting NASH may drive the liver to a more severe phenotype that resembles burnt-out NASH.
机译:微囊藻毒素-LR(MCLR)是一种肝毒性氰毒素,据报道会引起类似于非酒精性脂肪性肝炎(NASH)的表型。 NASH是一种常见的进行性肝病,由于外源性应激因素(例如不良饮食和有毒物质暴露)而导致严重性恶化。我们的目标是确定亚慢性MCLR毒性如何影响饮食引起的NASH。 Sprague-Dawley大鼠用以下三种饮食之一喂养10周:对照,蛋氨酸和胆碱缺乏症(MCD)或高脂肪/高胆固醇(HFHC)。饮食六周后,动物每隔一天腹膜内注射媒介物,10 µg / kg或30 µg / kg MCLR,在最后4周中。组织病理学终点的发生率和严重程度评分表明,MCLR毒性使NASH变为脂肪少,纤维化程度更高的状态。通常,涉及新生脂肪形成和脂肪酸酯化的基因的表达被改变,以减少脂肪变性。较高的MCLR剂量会增加对照组和HFHC组中涉及纤维化和炎症的基因的表达。这些数据表明,在已存在NASH的情况下,MCLR毒性可能将肝脏驱动为更严重的表型,类似于烧坏的NASH。

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